945762-00-5 Usage
General Description
3-bromo-1H-indazole-7-carbonitrile is a chemical compound that belongs to the indazole family. It is a derivative of indazole with a bromine atom and a cyano group attached to its 7th carbon. 3-bromo-1H-indazole-7-carbonitrile is widely used in pharmaceutical research, especially in the development of new drug molecules due to its unique chemical structure and potential pharmacological properties. It has been found to exhibit various biological activities and has potential applications in the synthesis of novel pharmaceuticals and organic compounds. The chemical properties and reactivity of 3-bromo-1H-indazole-7-carbonitrile make it a valuable building block in the synthesis of complex organic molecules and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 945762-00-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,7,6 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 945762-00:
(8*9)+(7*4)+(6*5)+(5*7)+(4*6)+(3*2)+(2*0)+(1*0)=195
195 % 10 = 5
So 945762-00-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H4BrN3/c9-8-6-3-1-2-5(4-10)7(6)11-12-8/h1-3H,(H,11,12)
945762-00-5Relevant articles and documents
INDOLE COMPOUNDS AS ANDROGEN RECEPTOR MODULATORS
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Page/Page column 40; 159, (2022/02/05)
Provided herein are compounds of formula (V) that bind to BF3 of an androgen receptor (AR), which can modulate the AR for the treatment of Kennedy's disease.
Efficient synthesis of 7-substituted or 3,7-disubstituted 1H-indazoles
Cottyn, Betty,Vichard, Dominique,Terrier, Fran?ois,Nioche, Pierre,Raman
, p. 1203 - 1206 (2008/01/08)
This work reports on the synthesis of the novel indazole scaffolds 7-OTf-1H-indazole (trifluoromethanesulfonic acid 1H-indazol-7-yl ester), 7-iodo-1H-indazole and 3-bromo-7-iodo-1H-indazole. These new compounds are potent building blocks in divergent syntheses of indazoles via palladium cross-coupling reactions. Georg Thieme Verlag Stuttgart.